MSH6 c.1309C>T ;(p.H437Y)

Variant ID: 2-48026431-C-T

NM_000179.2(MSH6):c.1309C>T;(p.H437Y)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A comprehensive evaluation of pathogenic mutations in primary cutaneous melanomas, including the identification of novel loss-of-function variants.

Scientific Reports
Ticha, Ivana I; Hojny, Jan J; Michalkova, Romana R; Kodet, Ondrej O; Krkavcova, Eva E; Hajkova, Nikola N; Nemejcova, Kristyna K; Bartu, Michaela M; Jaksa, Radek R; Dura, Miroslav M; Kanwal, Madiha M; Martinikova, Andra S AS; Macurek, Libor L; Zemankova, Petra P; Kleibl, Zdenek Z; Dundr, Pavel P
Publication Date: 2019-11-19

Variant appearance in text: MSH6: H437Y
PubMed Link: 31745173
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_53636.pdf
View BVdb publication page